Canonical Allele Identifier: CA401098804

Gene: UNC13D

Linked Data

• MyVariant Identifiers: chr17:g.73832318A>T (hg19) ; chr17:g.75836237A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75836237A>T , CM000679.2:g.75836237A>T	GRCh38
NC_000017.10:g.73832318A>T , CM000679.1:g.73832318A>T	GRCh37
NC_000017.9:g.71343913A>T	NCBI36
NG_007266.1:g.13481T>A , LRG_122:g.13481T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699510.1:c.344T>A	ENSP00000514405.1:p.Phe115Tyr
ENST00000699511.1:c.586T>A
ENST00000207549.9:c.1409T>A MANE Select	ENSP00000207549.3:p.Phe470Tyr
ENST00000207549.8:c.1409T>A	ENSP00000207549.3:p.Phe470Tyr
ENST00000412096.6:c.1409T>A	ENSP00000388093.1:p.Phe470Tyr
ENST00000586147.1:c.137T>A	ENSP00000466543.1:p.Phe46Tyr
ENST00000587105.1:c.528T>A
ENST00000591563.5:n.1679T>A
NM_199242.2:c.1409T>A , LRG_122t1:c.1409T>A	NP_954712.1:p.Phe470Tyr
XM_011524504.1:c.1409T>A	XP_011522806.1:p.Phe470Tyr
XM_011524505.1:c.1409T>A	XP_011522807.1:p.Phe470Tyr
XM_011524506.1:c.1406T>A	XP_011522808.1:p.Phe469Tyr
XM_011524507.1:c.800T>A	XP_011522809.1:p.Phe267Tyr
XM_011524508.1:c.800T>A	XP_011522810.1:p.Phe267Tyr
XM_011524504.2:c.1409T>A	XP_011522806.1:p.Phe470Tyr
XM_011524507.2:c.800T>A	XP_011522809.1:p.Phe267Tyr
XM_024450640.1:c.800T>A	XP_024306408.1:p.Phe267Tyr
NM_199242.3:c.1409T>A MANE Select	NP_954712.1:p.Phe470Tyr